scholarly journals Genomic expression differences between cutaneous cells from red hair color individuals and black hair color individuals based on bioinformatic analysis

Oncotarget ◽  
2016 ◽  
Vol 8 (7) ◽  
pp. 11589-11599 ◽  
Author(s):  
Joan Anton Puig-Butille ◽  
Pol Gimenez-Xavier ◽  
Alessia Visconti ◽  
Jérémie Nsengimana ◽  
Francisco Garcia-García ◽  
...  
2017 ◽  
Author(s):  
P. Frost ◽  
K. Kleisner ◽  
J. Flegr

AbstractBackgroundRed hair is associated with pain sensitivity, and more so in women than in men. Hair redness may thus interact with a female-specific factor. We tested this hypothesis on a large sample of Czech and Slovak respondents. They were asked about the natural redness and darkness of their hair, their natural eye color, their physical and mental health (24 categories), and other personal attributes (height, weight, number of children, lifelong number of sexual partners, frequency of smoking).ResultsWe found that red-haired women did worse than other women in ten health categories and better in only three. In particular, they were more prone to colorectal, cervical, uterine, and ovarian cancer. Cancer risk increased steadily with increasing hair redness except for the reddest shade. Red-haired men showed a balanced pattern of health effects, doing better than other men in three categories and worse in three. Number of children was the only category where both male and female redheads did better than other respondents. We also confirmed earlier findings that red hair is naturally more frequent in women than in men.ConclusionRed-haired women had higher fecundity and sexual attractiveness, but this selective advantage seems offset by worse health outcomes and therefore lower viability. The resulting equilibrium between these two counterbalancing forces might explain why red hair has remained less common than other hair and eye colors. Of the ‘new’ hair and eye colors, red hair diverges the most from the ancestral state of black hair and brown eyes. It is the most sexually dimorphic variant, not only in population frequency but also in health outcomes. This sexual dimorphism seems to have resulted from a selection pressure that acted primarily on early European women and which led to a general and apparently rapid diversification of hair and eye colors.


2013 ◽  
Vol 821-822 ◽  
pp. 28-31
Author(s):  
Yuan Chen ◽  
Qiong Li ◽  
Wan Ping Zhang ◽  
Jian Jie Cui ◽  
Xiao Jian Wu

Color protective effects of honeysuckle extract, benzophenone-3, and non-ionic silicon emulsion to hair fibers were compared by measuring color change of hair exposed to UV irradiation. Dyed color fades faster than natural pigment of hair after sunlight irradiation. Experiment results indicate that honeysuckle extract prevented color fading of dyed red hair in 49.52% and virgin black hair in 19.35% due to its strong antioxidant ability, while color protection effect of benzophenone-3 is not obvious. Non-ionic silicone emulsion provided the best maintenance of hair color of 81.46% in dyed red hair and 41.94% in virgin black hair. However, the synergy of honeysuckle extract with non-ionic silicone emulsion for hair color protecting was not encouraged.


2021 ◽  
Author(s):  
Elizabeth Tapanes ◽  
Rachel L. Jacobs ◽  
Ian Harryman ◽  
Edward E. Louis ◽  
Mitchell T. Irwin ◽  
...  

Hair (i.e., pelage/fur) is a salient feature of primate (including human) diversity and evolution-serving functions tied to thermoregulation, protection, camouflage, and signaling-but wild primate pelage biology and evolution remain relatively understudied. Specifically, assessing multiple hypotheses across distinct phylogenetic scales is essential but is rarely conducted. We examine whole body hair color and density variation across the Indriidae lemurs (Avahi, Indri, Propithecus)-a lineage that, like humans, exhibits vertical posture (i.e., their whole bodies are vertical to the sun). Our analyses consider multiple phylogenetic scales (family-level, genus-level) and hypotheses (e.g., Gloger's rule, the body cooling hypotheses). Our results show that across the Indriidae family, darker hair is typical in wetter regions (per Gloger's rule). However, within Propithecus, dark black hair is common in colder forest regions, which may implicate thermoregulation and is the first empirical evidence of Bogert's rule in mammals. Results also show pelage redness increases in populations exhibiting enhanced color vision and may thus aid conspecific communication in forested environments. Lastly, across Indriidae, we find follicle density on the crown and limbs increases in dry and open environments-rare empirical evidence supporting an early hypothesis on hominin hair evolution. We find an effect of body size on hue (red hair) and hair density but not on brightness (black hair). This study highlights how different selective pressures across distinct phylogenetic scales have likely acted on primate hair evolution. Lastly, since hair does not fossilize, the results of follicle and hair density variation across this clade offer us some potential insight into contextualizing human hair evolution.


Author(s):  
Muhammad Wasim ◽  
Haq N. Khan ◽  
Hina Ayesha ◽  
Mazhar Iqbal ◽  
Abdul Tawab ◽  
...  

Abstract Background Classical homocystinuria (HCU) is an autosomal recessive inborn error of metabolism, which is caused by the cystathionine-β-synthase (CBS: encoded by CBS) deficiency. Symptoms of untreated classical HCU patients include intellectual disability (ID), ectopia lentis and long limbs, along with elevated plasma methionine, and homocysteine. Methods A total of 429 ID patients (age range: 1.6–23 years) were sampled from Northern areas of Punjab, Pakistan. Biochemical and genetic analyses were performed to find classical HCU disease in ID patients. Results Biochemically, nine patients from seven unrelated families were identified with high levels of plasma methionine and homocysteine. Targeted exonic analysis of CBS confirmed seven causative homozygous mutations; of which three were novel missense mutations (c.451G>T; p.Gly151Trp, c.975G>C; p.Lys325Asn and c.1039 + 1G>T splicing), and four were recurrent variants (c.451 + 1G>A; IVS4 + 1 splicing, c.770C>T; p.Thr257Met, c.808_810del GAG; p.Glu270del and c.752T>C; p.Leu251Pro). Treatment of patients was initiated without further delay with pyridoxine, folic acid, cobalamin, and betaine as well as dietary protein restriction. The immediate impact was noticed in behavioral improvement, decreased irritability, improved black hair color, and socialization. Overall, health outcomes in this disorder depend on the age and symptomatology at the time of treatment initiation. Conclusions With personalized treatment and care, such patients can reach their full potential of living as healthy a life as possible. This screening study is one of the pioneering initiatives in Pakistan which would help to minimize the burden of such treatable inborn errors of metabolism in the intellectually disabled patients.


2019 ◽  
Vol 20 (11) ◽  
pp. 2665 ◽  
Author(s):  
Keiichi Hiramoto ◽  
Yurika Yamate ◽  
Yutaka Takishita ◽  
Eisuke F. Sato

We observed that on long-term breeding, gp91phox-knockout (gp91phox−/−) mice developed white hair. Here, we investigate the origin of this hitherto unexplained phenomenon. Moreover, we investigated the effect of tranexamic acid administration on the hair color in gp91phox−/− mice. We administered tranexamic acid (about 12 mg/kg/day) orally to 9-week-old C57BL/6j (control) and gp91phox−/− mice, thrice a week for 12 months. Compared to control mice, gp91phox−/− mice showed more white hair. However, the concentrations of reactive oxygen species and the levels of interleukin (IL)-1β and transforming growth factor (TGF)-β in the skin were lower than those in the control group. Furthermore, increase in white hair was observed in the control mice upon administration of the IL-1β antagonist. On the other hand, administration of tranexamic acid led to brown colored hair on gp91phox−/− mice. Although tranexamic acid treatment did not alter the expression levels of melanocortin receptor 1 and agouti signaling protein on hair follicles, it increased the expression of mahogunin ring finger protein 1 (MGRN1) and collagen XVII. These results suggested that retention of black hair requires the gp91phox/ROS/IL-1β/TGF-β pathway and that elevated levels of MGRN1 and collagen XVII lead to brown hair in gp91phox−/− mice.


2008 ◽  
Vol 215 (2) ◽  
pp. 344-355 ◽  
Author(s):  
Donald W. Roberts ◽  
Richard A. Newton ◽  
J. Helen Leonard ◽  
Richard A. Sturm
Keyword(s):  

2009 ◽  
Vol 140 (7) ◽  
pp. 896-905 ◽  
Author(s):  
Catherine J. Binkley ◽  
Abbie Beacham ◽  
William Neace ◽  
Ronald G. Gregg ◽  
Edwin B. Liem ◽  
...  

2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Yingjin Qiao ◽  
Anna-Lena Berg ◽  
Pei Wang ◽  
Yan Ge ◽  
Songxia Quan ◽  
...  

Abstract Melanocortin therapy by using adrenocorticotropic hormone (ACTH) or non-steroidogenic melanocortin peptides attenuates proteinuria and glomerular injury in experimental glomerular diseases and induces remission of nephrotic syndrome in patients with diverse glomerulopathies, even those resistant to steroids. The underlying mechanism remains elusive, but the role of melanocortin 1 receptor (MC1R) has been implicated and was examined here. Four patients with congenital red hair color and nephrotic syndrome caused by idiopathic membranous nephropathy or focal segmental glomerulosclerosis were confirmed by gene sequencing to bear dominant-negative MC1R mutations. Despite prior corticosteroid resistance, all patients responded to ACTH monotherapy and ultimately achieved clinical remission, inferring a steroidogenic-independent and MC1R-dispensable anti-proteinuric effect of melanocortin signaling. In confirmatory animal studies, the protective effect of [Nle4, D-Phe7]-α-melanocyte stimulating hormone (NDP-MSH), a potent non-steroidogenic pan-melanocortin receptor agonist, on the lipopolysaccharide elicited podocytopathy was completely preserved in MC1R-null mice, marked by reduced albuminuria and diminished histologic signs of podocyte injury. Moreover, in complementary in vitro studies, NDP-MSH attenuated the lipopolysaccharide elicited apoptosis, hypermotility and impairment of filtration barrier function equally in primary podocytes derived from MC1R-null and wild-type mice. Collectively, our findings suggest that melanocortin therapy confers a proteinuria reducing and podoprotective effect in proteinuric glomerulopathies via MC1R-independent mechanisms.


2013 ◽  
Vol 5 ◽  
pp. BIC.S12754 ◽  
Author(s):  
Per A. Andresen ◽  
Dag A. Nymoen ◽  
Kristina Kjærheim ◽  
Torbjørn Leivestad ◽  
Per Helsing

The highly polymorphic melanocortin 1 receptor ( MC1R) gene plays a crucial role in pigmentation. Variants of the gene have been implicated in risk of cutaneous squamous cell carcinoma (SCC) in the general population. In renal transplant (RT) recipients these cancers are more aggressive and very common. To evaluate the risk of SCC relative to MC1R and the pigmentation-associated genes ASIP, TYR, and TYRP1, a group of 217 RT recipients with and without SCC was genotyped. Associations with SCC risk were indicated in carriers of the red hair color associated MC1R variant p.Arg151Cys (OR= 1.99; 1.05–-3.75), and in carriers of two of any of the MC1R variants disclosed (OR = 2.36; 1.08–5.15). These associations appeared independent of traditionally protective phenotypes, also supported by the stratifications from skin phototype and hair color. A tendency towards an increased SCC risk was observed for a specific ASIP haplotype (OR = 1.87; 0.91–3.83), while no such associations were observed for the TYR and TYRP1 variants. Thus, the risk of developing SCC in RT patients is modulated by MC1R variation irrespective of phenotypes considered to be protective. Heterozygous combinations of MC1R variants appear to be more relevant in assessing SCC risk than the effects of variants individually.


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